Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886037936
rs886037936
EML1
0.800 GeneticVariation UNIPROT The genetic landscape of familial congenital hydrocephalus. 28556411

2017
dbSNP: rs886037937
rs886037937
EML1
0.800 GeneticVariation UNIPROT The genetic landscape of familial congenital hydrocephalus. 28556411

2017
dbSNP: rs886037936
rs886037936
EML1
0.800 GeneticVariation UNIPROT Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human. 24859200

2014
dbSNP: rs886037937
rs886037937
EML1
0.800 GeneticVariation UNIPROT Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human. 24859200

2014
dbSNP: rs886037936
rs886037936
EML1
G 0.800 CausalMutation CLINVAR

dbSNP: rs886037937
rs886037937
EML1
C 0.800 CausalMutation CLINVAR

dbSNP: rs1555404109
rs1555404109
EML1
T 0.700 CausalMutation CLINVAR

dbSNP: rs886037935
rs886037935
EML1
T 0.700 CausalMutation CLINVAR